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Merck

381071

Sigma-Aldrich

2-Aminoterephthalic acid

99%

Sinónimos:

2-Aminobenzene-1,4-dicarboxylic acid

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About This Item

Fórmula lineal:
H2NC6H3-1,4-(CO2H)2
Número de CAS:
Peso molecular:
181.15
Beilstein/REAXYS Number:
2805625
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

powder, crystals or chunks

reaction suitability

reaction type: solution phase peptide synthesis

mp

324 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cc(ccc1C(O)=O)C(O)=O

InChI

1S/C8H7NO4/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3H,9H2,(H,10,11)(H,12,13)

InChI key

GPNNOCMCNFXRAO-UHFFFAOYSA-N

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Application

2-Aminoterephthalic acid can be used to synthesize:
  • Lanthanide coordination polymers with 1,10-phenanthroline by hydrothermal method.
  • Blue-emitting derivatives of 2-aminoterephthalic acid.
  • Amino-functionalized Zr-terephthalate (UiO-66), an excellent catalyst for selective synthesis of jasminaldehyde.
  • IRMOF-3, a zinc aminoterephthalate metal-organic framework useful as a catalyst for the Knoevenagel condensation of benzaldehyde and ethyl cyanoacetate.
  • Polymeric composite membrane with excellent CO2 separation capabilities.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Los clientes también vieron

An amino-modified Zr-terephthalate metal?organic framework as an acid?base catalyst for cross-aldol condensation
Vermoortele F, et al.
Chemical Communications (Cambridge, England), 47(5), 1521-1523 (2011)
Weiwei Zhao et al.
PloS one, 12(6), e0178513-e0178513 (2017-06-06)
UiO-66 analogues are good candidates as stationary phase in HPLC because of their chemical/thermal stability, large surface area, and two cage structures. Here, two UiO-66 analogues, UiO-66-NH2 and UiO-67, were synthesized and used as stationary phase in HPLC to evaluate
Hao Zhang et al.
Nanomaterials (Basel, Switzerland), 10(9) (2020-09-17)
A combination of calcination and hydrothermal processing was used to prepare a g-C3N4/UiO-66-NH2/CdS photocatalyst, and the degradation of tetracycline (TC) over this material was assessed. The photocatalytic performance of this nanocomposite was approximately 4.4 and 2.3 times those of CdS
Farhad Ahmadijokani et al.
Dalton transactions (Cambridge, England : 2003), 48(36), 13555-13566 (2019-07-30)
Mixed-matrix membranes (MMMs) are promising candidates for carbon dioxide separation. However, their application is limited due to improper dispersion of fillers within the polymer matrix, poor interaction of fillers with polymer chains, and formation of defects and micro-voids at the
Jianhao Qiu et al.
Chemosphere, 242, 125197-125197 (2019-11-02)
Industrial effluents often contain mixed metal ions and dyes, and it is difficult to efficiently remove both types of contaminants simultaneously. Here, MIL-125-NH2@Ag/AgCl composites were for the first time developed through a facile deposition-photoreduction method for simultaneously removing Cr(VI)/Rhodamine B

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